PMID- 36028823 OWN - NLM STAT- MEDLINE DCOM- 20220830 LR - 20220906 IS - 1471-2407 (Electronic) IS - 1471-2407 (Linking) VI - 22 IP - 1 DP - 2022 Aug 26 TI - Safety and efficacy profile of Trastuzumab deruxtecan in solid cancer: pooled reanalysis based on clinical trials. PG - 923 LID - 10.1186/s12885-022-10015-6 [doi] LID - 923 AB - PURPOSE: This study aimed to explore the efficiency and safety of the new generation antibody-drug conjugate Trastuzumab deruxtecan (DS-8201a) in treating HER2-positive solid cancers. METHOD: By searching PubMed, Medline and Ovid for all clinical trials related to the safety and efficacy of DS-8201a. Event rates were calculated for all adverse events (AEs) to evaluate the safety of DS-8201a. Objective response rate (ORR) and progression-free survival (PFS) were summarized to assess the potency of DS-8201a. RESULT: The AEs with event rates greater than 30% regardless of grades were nausea, decreased appetite, vomiting, fatigue, anemia, decreased neutrophil count, alopecia and diarrhea. In the grade 3 or more, decreased neutrophil count, anemia and decreased white blood cell count were the only three AEs with event rates greater than 10% (20.3, 15.0 and 10.3%). The median PFS of patients with breast cancer, gastric cancer and other HER2-positive solid cancers were 9.0-22.1, 3.0-8.3 and 4.1-11.9 months. The median ORR was 37-79.9% in patients with breast and gastric cancer and 28.3-55% in patients with other HER2-positive cancers. CONCLUSION: DS-8201a plays an active role in treating HER2-positive cancers, especially breast and gastric cancer, which have HER2 amplification. The most common AEs of DS-8201a were related to gastrointestinal and hematological system. Decreased white blood cell count and appetite were the AEs occurred with high grades. CI - (c) 2022. The Author(s). FAU - Xu, Hanyue AU - Xu H AD - Department of Biotherapy, West China Hospital and State Key Laboratory of Biotherapy, Sichuan University, Chengdu, 610041, Sichuan, P.R. China. AD - Department of Ophthalmology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, P.R. China. FAU - Zhang, Hao AU - Zhang H AD - Department of Pancreatic Surgery, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, P.R. China. FAU - Guo, Wen AU - Guo W AD - The Center of Gerontology and Geriatrics, West China Hospital, Sichuan University, Chengdu, 610041, PR China. FAU - Zhong, Xi AU - Zhong X AD - Department of Intensive Care Unit, West China HospitalSichuan University, Chengdu, 610041, PR China. FAU - Sun, Jing AU - Sun J AD - Integrated Traditional and Western Medicine Department, Qingdao Central Hospital, Qingdao University, Qingdao, Shandong, 266042, P.R. China. FAU - Zhang, Tao AU - Zhang T AD - Department of Biotherapy, West China Hospital and State Key Laboratory of Biotherapy, Sichuan University, Chengdu, 610041, Sichuan, P.R. China. FAU - Wang, Zhoufeng AU - Wang Z AD - Institute of Respiratory Health, Frontiers Science Center for Disease-Related Molecular Networks, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, P.R. China. wangzhoufeng@wchscu.cn. FAU - Ma, Xuelei AU - Ma X AD - Department of Biotherapy, West China Hospital and State Key Laboratory of Biotherapy, Sichuan University, Chengdu, 610041, Sichuan, P.R. China. drmaxuelei@gmail.com. LA - eng PT - Clinical Trial PT - Journal Article DEP - 20220826 PL - England TA - BMC Cancer JT - BMC cancer JID - 100967800 RN - 0 (Antibodies, Monoclonal, Humanized) RN - 0 (Immunoconjugates) RN - 5384HK7574 (trastuzumab deruxtecan) RN - EC 2.7.10.1 (Receptor, ErbB-2) RN - P188ANX8CK (Trastuzumab) RN - XT3Z54Z28A (Camptothecin) SB - IM MH - Antibodies, Monoclonal, Humanized MH - *Breast Neoplasms MH - Camptothecin/analogs & derivatives MH - Female MH - Humans MH - *Immunoconjugates MH - Receptor, ErbB-2 MH - *Stomach Neoplasms MH - Trastuzumab PMC - PMC9414434 OTO - NOTNLM OT - Adverse events OT - Breast cancer OT - Gastric cancer OT - Human epidermal growth factor receptor 2 OT - Progression free survival OT - Trastuzumab deruxtecan (DS-8201a) COIS- The authors declare that they have no competing interests. EDAT- 2022/08/27 06:00 MHDA- 2022/08/31 06:00 PMCR- 2022/08/26 CRDT- 2022/08/26 23:40 PHST- 2022/06/09 00:00 [received] PHST- 2022/08/10 00:00 [accepted] PHST- 2022/08/26 23:40 [entrez] PHST- 2022/08/27 06:00 [pubmed] PHST- 2022/08/31 06:00 [medline] PHST- 2022/08/26 00:00 [pmc-release] AID - 10.1186/s12885-022-10015-6 [pii] AID - 10015 [pii] AID - 10.1186/s12885-022-10015-6 [doi] PST - epublish SO - BMC Cancer. 2022 Aug 26;22(1):923. doi: 10.1186/s12885-022-10015-6.